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重要文件

I3631

Sigma-Aldrich

亚硝酸异戊酯

同義詞:

亚硝戊酯

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About This Item

線性公式:
(CH3)2CHCH2CH2ONO
CAS號碼:
分子量::
117.15
Beilstein:
969510
EC號碼:
MDL號碼:
分類程式碼代碼:
12171500
PubChem物質ID:

折射率

n20/D 1.386 (lit.)

bp

99 °C (lit.)

密度

0.872 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

CC(C)CCON=O

InChI

1S/C5H11NO2/c1-5(2)3-4-8-6-7/h5H,3-4H2,1-2H3

InChI 密鑰

OWFXIOWLTKNBAP-UHFFFAOYSA-N

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其他說明

This product has been replaced by 150495-Sigma-Aldrich | Isopentyl nitrite 96%

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產品號碼
描述
訂價

訊號詞

Danger

危險分類

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Muta. 2 - Skin Corr. 1B - Skin Sens. 1

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

-4.0 °F - closed cup

閃點(°C)

-20 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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分析證明 (COA)

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Rao M Uppu
Analytical biochemistry, 354(2), 165-168 (2006-06-06)
A method for the synthesis of peroxynitrite is described. It involves nitrosation of H2O2 at pH> or = 12.5 by isoamyl or butyl nitrite in mixed solvents of isopropyl alcohol (IPA) and water at 25+/-1 degrees C. Maximum yields of
Hossein Mehrabi
Ultrasonics sonochemistry, 15(4), 279-282 (2007-10-26)
The reaction of 6-acylmethylphenanthridines with isoamyl nitrite results alpha-oximino-6-acylmethylphenanthridines in 73-95% yields in DMF under ultrasound irradiation. Compared with conventional methods, the main advantages of the present procedure are milder conditions, shorter reaction time and higher yields.
Analysis of alkyl nitrites by capillary gas chromatography-mass spectrometry.
T S Bal et al.
Journal - Forensic Science Society, 28(3), 185-190 (1988-05-01)
R M Uppu et al.
Analytical biochemistry, 236(2), 242-249 (1996-05-01)
A new method for the preparation of high concentrations of peroxynitrite (up to 1 M) is described. The synthesis uses a two-phase system and involves a displacement reaction by the hydroperoxide anion (in the aqueous phase) on isoamyl nitrite (in
E Noack et al.
Basic research in cardiology, 86 Suppl 2, 37-50 (1991-01-01)
All nitrovasodilators act intracellularly by a common molecular mechanism. This is characterized by the release of nitric oxide (NO). They are, thus, prodrugs or carriers of the active principle NO, responsible for endothelial controlled vasodilation. The rate of NO-formation strongly

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